Latest papers

Structure, Dynamics, and Branch Migration of a DNA Holliday Junction: A Single-Molecule Fluorescence and Modeling Study

BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome.

RMI, a new OB-fold complex essential for Bloom syndrome protein to maintain genome stability.

Helix-coil transition of a four-way DNA junction observed by multiple fluorescence parameters.

The FANCM ortholog Fml1 promotes recombination at stalled replication forks and limits crossing over during DNA double-strand break repair.

Meeting DNA palindromes head-to-head.

Analysis of Strand Transfer and Template Switching Mechanisms of DNA Gap Repair by Homologous Recombination in Escherichiacoli: Predominance of Strand Transfer

[Molecular basis of the formation and branch migration of Holliday recombination intermediates mediated by eukaryotic recombinases]

The Werner syndrome protein binds replication fork and holliday junction DNAs as an oligomer.

The RecU Holliday junction resolvase acts at early stages of homologous recombination.

Interactions between branched DNAs and peptide inhibitors of DNA repair.

Rad51 protein stimulates the branch migration activity of Rad54 protein.

Chemistry. Halogen versus hydrogen.

Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis.

RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination.

AtRECQ2, a RecQ helicase homologue from Arabidopsis thaliana, is able to disrupt various recombinogenic DNA structures in vitro.

Single Molecule Fluorescence Analysis of Branch Migration of Holliday Junctions: Effect of DNA Sequence

Branch migration enzyme as a Brownian ratchet.

Functional role of BLAP75 in BLM-topoisomerase IIIalpha-dependent holliday junction processing.

DNA conformations and their sequence preferences.